Canonical Allele Identifier: CA382239296

Gene: DYNC2H1

Linked Data

• gnomAD v4: 11-103165896-A-G
• COSMIC: COSN1125421
• MyVariant Identifiers: chr11:g.103036625A>G (hg19) ; chr11:g.103165896A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103165896A>G , CM000673.2:g.103165896A>G	GRCh38
NC_000011.9:g.103036625A>G , CM000673.1:g.103036625A>G	GRCh37
NC_000011.8:g.102541835A>G	NCBI36
NG_016423.1:g.61466A>G
NG_016423.2:g.61466A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000650373.2:c.4612-2A>G MANE Plus Clinical	ENSP00000497174.1:n.4612-2A>G
ENST00000375735.7:c.4612-2A>G MANE Select	ENSP00000364887.2:n.4612-2A>G
ENST00000649323.1:c.*2157-2A>G	ENSP00000497581.1:n.*2157-2A>G
ENST00000650373.1:c.4612-2A>G	ENSP00000497174.1:n.4612-2A>G
ENST00000334267.11:c.2205+31477A>G	ENSP00000334021.7:n.2205+31477A>G
ENST00000375735.6:c.4612-2A>G	ENSP00000364887.2:n.4612-2A>G
ENST00000398093.7:c.4612-2A>G	ENSP00000381167.3:n.4612-2A>G
NM_001080463.1:c.4612-2A>G	NP_001073932.1:n.4612-2A>G
NM_001377.2:c.4612-2A>G	NP_001368.2:n.4612-2A>G
XM_006718903.2:c.4612-2A>G	XP_006718966.1:n.4612-2A>G
XM_017018291.1:c.4612-2A>G	XP_016873780.1:n.4612-2A>G
XM_017018292.1:c.3994-2A>G	XP_016873781.1:n.3994-2A>G
XM_017018293.1:c.4612-2A>G	XP_016873782.1:n.4612-2A>G
NM_001377.3:c.4612-2A>G MANE Select	NP_001368.2:n.4612-2A>G
NM_001080463.2:c.4612-2A>G MANE Plus Clinical	NP_001073932.1:n.4612-2A>G